| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:158644686-158644901 | Common:3; Rare:94 | ||||
| chr6:158818226-158818354 | Common:2; Rare:49 | ||||
| chr6:159726926-159727162 | Common:1; Rare:91 | ||||
| chr6:159727327-159727589 | Common:5; Rare:115 | ||||
| chr6:159762312-159762569 | Common:2; Rare:69 | ||||
| chr6:159789567-159789990 | Common:3; Rare:147 | ||||
| chr6:162727757-162727974 | Rare:58; Clinvar:1 | ||||
| chr6:163414646-163414811 | Rare:71 | ||||
| chr6:166342529-166342640 | Common:2; Rare:43 | ||||
| chr6:166999081-166999384 | Common:1; Rare:104 | ||||
| chr6:169701989-169702356 | Common:5; Rare:154 | ||||
| chr6:169751594-169751651 | Rare:28; Clinvar (benign):2 | ||||
| chr6:170306576-170306805 | Common:1; Rare:74 | ||||
| chr6:170584584-170584776 | Common:1; Rare:64 | ||||
| chr7:519154-519312 | Rare:40 |